Evidence map›Paper›PMID 42158853›Full record

ArticleFrontiers in immunology2026

Case Report: Treatment of refractory lung disease in systemic juvenile idiopathic arthritis with cyclophosphamide and rituximab combination therapy.

William J Freeman, Eileen C Rife, Randy Q Cron

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Article in Frontiers in immunology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

William J FreemanDepartment of General Pediatrics, Hofstra Northwell School of Medicine, Steven and Alexandra Cohen Children's Medical Center of New York, New Hyde Park, NY, United States.
Eileen C RifeDivision of Rheumatology, Department of Pediatrics, University of Alabama at Birmingham (UAB) Heersink School of Medicine, Children's of Alabama, Birmingham, AL, United States.
Randy Q CronDivision of Rheumatology, Department of Pediatrics, University of Alabama at Birmingham (UAB) Heersink School of Medicine, Children's of Alabama, Birmingham, AL, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Systemic juvenile idiopathic arthritis-associated lung disease (sJIA-LD) is a rare, potentially fatal complication of sJIA, often accompanied by pulmonary hypertension (PHTN) and macrophage activation syndrome (MAS). The underlying pathophysiology remains poorly understood and optimal management strategies have yet to be established. Recent retrospective data suggest that combination therapy with cyclophosphamide (CYC) and rituximab (RTX) may be effective in children with severe or life-threatening manifestations of rheumatic disease. Yet, literature on combination therapy in sJIA-LD is lacking. Methods: We describe two pediatric cases of sJIA-LD complicated by PHTN and recurrent episodes of MAS. Both patients remained refractory to conventional sJIA therapies, necessitating escalation with combination CYC-RTX. Results: Following combination CYC-RTX therapy, both patients demonstrated marked clinical improvement, including resolution of hyperferritinemia, normalization of acute phase reactants, and recovery of hepatic function profiles. Patient 1 experienced a reduction in supplemental oxygen requirement from 4 liters per minute (LPM) to 0.5 LPM nocturnally as well as improved PHTN measures: mean pulmonary arterial pressure decreased from 47 to 25 mmHg, and pulmonary vascular resistance decreased from 11.1 to 4.3 Wood units. Patient 2 experienced improved height velocity from <3rd percentile to >10th percentile and weaned off all therapies. Daily prednisone requirement for patient 1 decreased from 1 to <0.2 mg/kg/day. Chest computed tomography showed notable improvements in ground-glass opacities and septal and pleural thickening in both patients. Conclusion: Combination therapy with CYC and RTX may represent a valuable therapeutic approach in refractory sJIA complicated by lung disease, particularly in patients with concomitant MAS or PHTN.

Indexed as

Antirheumatic AgentsArthritis, JuvenileCyclophosphamideHypertension, PulmonaryLung DiseasesRituximabChildDrug Therapy, CombinationFemaleHumansMacrophage Activation SyndromeMaleTreatment OutcomeAntirheumatic AgentsCyclophosphamideRituximabcase reportcombination therapycyclophosphamidelung diseasemacrophage activation syndromepulmonary hypertensionrituximabsystemic juvenile idiopathic arthritis

Identifiers

PMID42158853
PMCPMC13180542

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.